HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666722Generated: November 1, 2026
Aniline → 1-(Phenylamino)cyclopentanecarbonitrile
https://huagongshe.com/reaction/1666722
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Cyclopentanone | HCID 8452 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1-(Phenylamino)cyclopentanecarbonitrile | HCID 243095 | 91.3% |
Reaction Steps
2.9 ml (31.8 mmol) of aniline (starting product 2) are added to a solution of 2.6 ml (29.4 mmol) of cyclopentanone (starting product 3) in 30 ml of acetic acid at 0° C. The solution is stirred for 15 minutes and 4 ml (30 mmol) of trimethylsilyl cyanide are added. The reaction medium is stirred for one night at room temperature and then gently poured into an ice-cold ammonium hydroxide solution while keeping the pH basic and extracted with dichloromethane. The organic phases are collected and washed with water. They are dried over sodium sulfate. The solvents are evaporated and then the residue is chromatographed on silica gel (heptane/ethyl acetate 90/10, v/v). 5 g of 1-phenylaminocyclopentanecarbonitrile are obtained in the form of a clear brown oil. Yield=91%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044082B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-4230310b57dd42d9bc8375e311f011df |
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| Source note | uspto-grants-2011_10 |
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